Hemochromatosis in a β-thalassemia minor patient with H63D homozygous mutation: A case report.
Nishan Babu PokhrelShambhu KhanalParikshit ChapagainBiraj PokhrelAnjan ShresthaPublished in: Clinical case reports (2020)
β-thalassemia heterozygosity can cause significant iron overload when accompanied by HFE gene mutations and inappropriate iron supplementation.